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Isabel Filges

Showing results (1-10 of 62) with videos related to

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Molecular Syndromology|December 13, 2021
Gene Ontology Enrichment Analysis of Renal Agenesis: Improving Prenatal Molecular DiagnosisSilvia Kalantari, Isabel Filges
European Journal of Human Genetics : EJHG|September 7, 2019
CUGC for Stromme syndrome and CENPF-related disordersIsabel Filges, Petter Stromme
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|February 7, 2023
Fetal hyperechogenic kidneys: the significance of family assessmentSevgi Tercanli, Isabel Filges
Journal of Medical Genetics|May 21, 2020
'Kinesinopathies': emerging role of the kinesin family member genes in birth defectsSilvia Kalantari, Isabel Filges
Prenatal Diagnosis|January 9, 2013
Failure to identify antenatal multiple congenital contractures and fetal akinesia--proposal of guidelines to improve diagnosisIsabel Filges, Judith G Hall
Prenatal Diagnosis|July 22, 2014
Exome sequencing for gene discovery in lethal fetal disorders--harnessing the value of extreme phenotypesIsabel Filges, Jan M Friedman
Prenatal Diagnosis|August 1, 2012
We are failing to identify disorders of fetal movement--why?Isabel Filges, Judith G Hall
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|January 14, 2016
Increased Fetal Nuchal Translucency - Also a Risk for a Rare Submicroscopic Chromosomal AbnormalitiesSevgi Tercanli, Peter Miny, Isabel Filges
Prenatal Diagnosis|May 26, 2017
A novel homozygous splice-site mutation in RYR1 causes fetal hydrops and affects skeletal and smooth muscle developmentNicole Meier, Elisabeth Bruder, Isabel Filges
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|July 19, 2019
Fetal arthrogryposis: Challenges and perspectives for prenatal detection and managementIsabel Filges, Sevgi Tercanli, Judith G Hall
Pageof 7

Showing results (1-10 of 62) with videos related to

Sort By:
Pageof 7
Molecular Syndromology|December 13, 2021
Gene Ontology Enrichment Analysis of Renal Agenesis: Improving Prenatal Molecular DiagnosisSilvia Kalantari, Isabel Filges
European Journal of Human Genetics : EJHG|September 7, 2019
CUGC for Stromme syndrome and CENPF-related disordersIsabel Filges, Petter Stromme
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|February 7, 2023
Fetal hyperechogenic kidneys: the significance of family assessmentSevgi Tercanli, Isabel Filges
Journal of Medical Genetics|May 21, 2020
'Kinesinopathies': emerging role of the kinesin family member genes in birth defectsSilvia Kalantari, Isabel Filges
Prenatal Diagnosis|January 9, 2013
Failure to identify antenatal multiple congenital contractures and fetal akinesia--proposal of guidelines to improve diagnosisIsabel Filges, Judith G Hall
Prenatal Diagnosis|July 22, 2014
Exome sequencing for gene discovery in lethal fetal disorders--harnessing the value of extreme phenotypesIsabel Filges, Jan M Friedman
Prenatal Diagnosis|August 1, 2012
We are failing to identify disorders of fetal movement--why?Isabel Filges, Judith G Hall
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|January 14, 2016
Increased Fetal Nuchal Translucency - Also a Risk for a Rare Submicroscopic Chromosomal AbnormalitiesSevgi Tercanli, Peter Miny, Isabel Filges
Prenatal Diagnosis|May 26, 2017
A novel homozygous splice-site mutation in RYR1 causes fetal hydrops and affects skeletal and smooth muscle developmentNicole Meier, Elisabeth Bruder, Isabel Filges
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|July 19, 2019
Fetal arthrogryposis: Challenges and perspectives for prenatal detection and managementIsabel Filges, Sevgi Tercanli, Judith G Hall
Pageof 7